Home NDC 84562-871 Tanning Club Everyday Sunscreen SPF 30
Product NDC 84562-871
11-digit product format 845620871
Labeler code 84562
Product ID 84562-871_3bb35608-bd81-8d78-e063-6294a90a0d86
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE
Dosage form LOTION
Route TOPICAL
Labeler TANNING CLUB, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-28
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE
Active strength 100; 50; 50; 30 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Tanning Club Everyday Sunscreen SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 50 mg/mL AVOBENZONE 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84562-871-00 Tanning Club Everyday Sunscreen SPF 30 170 mL in 1 BOTTLE LOTION 170 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84562-871-00 84562087100 170 mL in 1 BOTTLE (84562-871-00) 170 ml 2025-07-28 No No Current